[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100410367":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":22,"locations":28,"responsibleParty":52,"collaborators":10,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":10,"enrollmentInfo":63,"targetDuration":66,"studyType":67,"phases":10,"briefSummary":68,"conditions":69,"keywords":10,"overallStatus":31,"whyStopped":10,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Universitaire Ziekenhuizen KU Leuven","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Inguinal or femoral hernia repair",null,"All consecutive inguinal or femoral hernia repair (primary or mesh)",[13],"Device: Surgical inguinal or femoral hernia repair",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","Surgical inguinal or femoral hernia repair","Surgical inguinal or femoral hernia repair (primary or mesh)",[9],[21],"Hernia repair",[23],{"name":24,"role":25,"phone":26,"phoneExt":10,"email":27},"Colette Ms. Barlé","CONTACT","++32 16 341699","colette.barle@uzleuven.be",[29,48],{"facility":30,"status":31,"city":32,"state":10,"zip":33,"country":34,"countryCode":35,"cosmosGeoPoint":36,"geoPoint":41,"contacts":42},"UZ Leuven","RECRUITING","Leuven","3000","Belgium","BE",{"type":37,"coordinates":38},"Point",[39,40],4.70093,50.87959,{"lat":40,"lon":39},[43,45],{"name":44,"role":25,"phone":26,"phoneExt":10,"email":27},"Colette Barlé",{"name":46,"role":47,"phone":10,"phoneExt":10,"email":10},"Marc Miserez, Prof.Dr.","PRINCIPAL_INVESTIGATOR",{"facility":44,"status":31,"city":32,"state":10,"zip":10,"country":34,"countryCode":35,"cosmosGeoPoint":49,"geoPoint":51,"contacts":10},{"type":37,"coordinates":50},[39,40],{"lat":40,"lon":39},{"type":53,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100410367","flemish-inguinal-and-femoral-hernia-prospective-registry-100410367",false,"NCT04623580","Flemish Inguinal and Femoral Hernia Prospective Registry","FLIPR","Inclusion criteria\n\n* Consecutively all patients with a groin hernia (inguinal and\u002For femoral hernia) operated starting 01.01.2018.\n* Male and female\n* 18 years or older\n* Operated of supervised by a participating surgeon (participating in this study is not necessarily by a whole surgical department of a hospital, but by specific surgeons)\n* Elective and emergency surgery\n* Primary and recurrent hernia\n* Metachronous and synchronous hernia\n* Signed informed consent form\n\nExclusion criteria\n\n* Younger than 18 years\n* Not operated or supervised by participating surgeon\n* Pregnant at inclusion in the registry\n* No signed informed consent form","ALL","18 Years",{"count":64,"type":65},560,"ESTIMATED","5 Years","OBSERVATIONAL","Prospective registry. The purpose of this clinical trial will be to measure surgical outcome parameters (e.g. recurrence, chronic pain and other quality indicators) after inguinal hernia repair using Patient Reported Outcome Measures (PROMs) in the short- and long-term.",[70],"Inguinal Hernia","2024-06-28",{"date":73,"type":74},"2024-07-01","ACTUAL",{"date":76,"type":74},"2018-01-01",{"date":78,"type":65},"2028-12-31",{"name":5,"class":6},2]